- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …areas centered around rare diseases and immune disorders. Summary Position supports safety monitoring and risk management activities, provides insights on current ... clinical practice and guidelines, reviews and provides written assessments...position supports a senior physician in evaluating and mitigating safety signals as they arise. Additionally, this position works… more
- Merck & Co. (Rahway, NJ)
- …new milestones in global healthcare. Our company's Pharmaceutical Sciences & Clinical Supplies organization translates molecules to medicines, working from the ... a range of modalities including small molecules and peptides.- Within OFS, the Director will influence the strategy, lead activities, and develop a team whose roles… more
- Merck & Co. (Rahway, NJ)
- …The FLEx Co-Lead role is based in New Jersey and reports to the Associate Vice President of Pharmaceutical Operations and Clinical Supply in our Research ... Job DescriptionFLEx is a set of multi-modality Drug Product development and GMP clinical manufacturing assets being constructed in the Rahway, New Jersey site, to… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …equal opportunity employer including veterans and people with disabilities. Summary The Associate Director , External Data Management, is accountable for the ... of External data in Daiichi Sankyo R&D collaborating with clinical and medical teams, clinical safety and pharmacovigilance, CROs and External Vendors… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …areas centered around rare diseases and immune disorders. SUMMARYThe Associate Director , Pharmacoepidemiology position provides epidemiologic, methodological, ... journalsAssess clinical trial and/or other data sources to contextualize safety events for assigned product. Research natural history of disease to characterize… more
- Merck & Co. (Rahway, NJ)
- …effective, innovative medicine.The Global Clinical Data Standards Vocabulary Specialist, Associate Director , is a subject matter expert in CDISC Controlled ... boundaries of global healthcare through research and innovation. Through clinical trials and surveillance, we ensure the safety... clinical trials and surveillance, we ensure the safety and efficacy of our existing and pipeline products… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …develop programming submission strategy, perform integrated analysis of efficacy and safety , generate submission data package, create TLFs to support submission QAs, ... perform ad-hoc and exploratory analysis requested by clinical team, and support agency response or potential Advisory Committee Meeting- Develop DSI programming… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …and those involving 3rd party development. This position partners with GRLs and Clinical Safety Pharmacovigilance (CSPV) leads in the maintenance of Company Core ... Data Sheets (CCDS) for assigned products. This position drives/leads the maintenance of global labeling and associated documents (including cartons and external packaging in the US) for assigned Daiichi Sankyo products. This position ensures that draft… more
- Mercy University (Dobbs Ferry, NY)
- Nursing Associate Director of Clinical Simulation Lab Print (https://www.schooljobs.com/careers/mercyedu/jobs/newprint/4377897) Apply Nursing Associate ... Non-Union + Description + Benefits Job Posting Summary The Associate Director of the Clinical ...medical skills learning lab. Recent medical surgical experience. + Safety standards and practices used in lab/classroom settings. Education… more
- Bristol Myers Squibb (Summit, NJ)
- …at work and in their personal lives. Read more: careers.bms.com/working-with-us . The Associate Director , EHS, Safety & Incident Management position will ... the Environment, Occupational Health, Safety and Sustainability (EOHSS) Department. The Associate Director is the Subject Matter Expert (SME) for Environment… more
- Intra-Cellular Therapies, Inc (New York, NY)
- …national origin, protected veteran status, disability or any other legally protected status. Associate Director Clinical Development Base Salary range $175K ... respect in all we do, create and deliver. The Associate Director / Director Clinical ...as primary contact for medical communication to ensure medical safety within studies. Develop and maintain relationships with sites… more
- Bristol Myers Squibb (Madison, NJ)
- …such as the /Company Core Data Sheet (CCDS)/ label, Briefing book and Summary of clinical safety . + Author HA safety query responses + Contributes to ... Report drafting a preliminary conclusion. + Develops strategies for safety data collection in clinical trials to...Develops strategies for safety data collection in clinical trials to further characterize adverse events of interest.… more
- Pfizer (Pearl River, NY)
- …into country feasibility. **Support study team** + With supervision of medical monitor ( director /Sr director ) provides clinical input to protocol/study team ... Contributes to medical review and interpretation of efficacy and safety data from clinical trials; this includes...+ Provides protocol specific training to study team, investigators, clinical research associate , and others. + Interacts… more
- City of New York (New York, NY)
- …of Public Health Laboratories seeks a qualified candidate to serve as an Associate Director . This position will report to the Assistant Commissioner/ Laboratory ... safety of New York City residents by providing clinical and environmental laboratory testing services. With more than...and direct supervision of Laboratory Unit Chiefs. Additionally, the Associate Director will contribute to the vision… more
- Pfizer (Pearl River, NY)
- …of accountability for design, execution, monitoring, delivery and reporting of one or more clinical studies and to ensure patient safety . + The clinician medical ... + Conducts medical review and interpretation of efficacy and safety data from clinical trials; this may...+ Provides protocol specific training to study team, investigators, clinical research associate , and others. + Interacts… more
- Bristol Myers Squibb (New York, NY)
- …in their personal lives. Read more: careers.bms.com/working-with-us . **Summary** The Regional Associate Director (RAD) role is field-based and focused on ... support of BMS medicines and all phases of associated clinical trials. The RAD oversees their regional team to...timelines + Contributes to managing external communication when significant safety issues arise, with the well-being of patients being… more
- Bristol Myers Squibb (Berkeley Heights, NJ)
- …every treatment we pioneer. Join us and make a difference. **Purpose** The Associate Director , Biostatistics is a core member of cross-functional development ... the development and execution of statistical aspects for one or more clinical trials, including contribution to study trial design, analysis planning, study results… more
- The Mount Sinai Health System (New York, NY)
- … safety aspects of clinical research trial(s). Under guidance of the Associate Director of Research and Quality Outcomes, the CRA is responsible for ... The Clinical Research Associate is an integral...The Clinical Research Associate is an integral part of the research...collecting, assessing and processing Adverse Events (SAE) for safety reporting, CEC and DSMB of clinical … more
- NYU Rory Meyers College of Nursing (New York, NY)
- Position Summary The Associate Director of Dining acts as a Dining Services strategic liaison for facilities-related issues, equipment issues, purchases, and ... EOE/AA/Minorities/Females/Vet/Disabled/Sexual Orientation/Gender Identity Share this job (https://uscareers-nyu.icims.com/jobs/13303/ associate - director -of-dining/job?mode=apply&apply=yes&in\_iframe=1&hashed=-336115631) Need help finding… more
- Bristol Myers Squibb (Madison, NJ)
- …their personal lives. Read more: careers.bms.com/working-with-us . **Summary:** The role of Associate Director of US Commercial Regulatory Affairs requires the ... institutional campaigns. + Proven aptitude to analyze and interpret efficacy and safety data. + Experience communicating and negotiating with OPDP/APLB is a plus.… more
